Senior Principal Investigator, Clinical Trials

ActivMed Practices & Research, LLC.; Katy (TX); On-site; USD 180,000 - 260,000; Full time

Benefits offered by this job

Health insurance

Dental insurance

Vision insurance

401k plan

Paid time off

Job summary

Alcanza Clinical Research is seeking a Principal Investigator to lead daily clinical trial activities across multiple locations, ensuring patient safety and protocol compliance per ICH/FDA/GCP guidelines.

The ideal candidate holds an MD or DO with an active license, board certification, and at least 2 years of medical research experience, with CPR mandatory and ACLS preferred. This is a full-time, site-based role with broad collaboration across sponsors and staff.

Qualifications

• MD or DO degree with active physician license in good standing
• Board certification in area of specialty required
• CPR required; ACLS preferred
• Minimum 2 years of experience in a medical research environment or equivalent education/experience

Responsibilities

• Ensure medical well-being and safety of participants per FDA/ICH/GCP and HIPAA guidelines
• Provide overall site leadership to enhance efficiencies and compliance
• Evaluate participant eligibility for enrollment in trials
• Facilitate participant delivery and retention of studies
• Collaborate with sponsors, clients and team members
• Maintain accurate data recording and protocol adherence
• Participate in investigator meetings and ongoing training
• Perform other duties as assigned as needed

Skills

Clinical skills

MS Office

Electronic health records

Typing speed

Organizational skills

Bilingual English/Spanish

Interpersonal skills

Multitasking

HIPAA compliance

Independent work

Education

MD or DO with board certification

Tools

Electronic Health Records (EHR) systems

Job description

Alcanza Clinical Research is seeking a Principal Investigator to lead daily clinical trial activities across multiple locations, ensuring patient safety and protocol compliance per ICH/FDA/GCP guidelines.

The ideal candidate holds an MD or DO with an active license, board certification, and at least 2 years of medical research experience, with CPR mandatory and ACLS preferred. This is a full-time, site-based role with broad collaboration across sponsors and staff.